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IAVI and Merck Collaborate to Develop Vaccine Against SARS-CoV-2
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Merck to Acquire Themis
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Merck (MRK) will today announce three significant scientific initiatives to combat COVID-19
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Merck to Announce Multiple Scientific Efforts to Combat COVID-19
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Merck (MRK), AstraZeneca (AZN) Report LYNPARZA (olaparib) Approved by FDA for Treatment of HRR Gene-Mutated Metastatic Castration-Resistant Prostate Cancer
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LYNPARZA® (olaparib) Approved by FDA for Treatment of HRR Gene-Mutated Metastatic Castration-Resistant Prostate Cancer That Has Progressed Following Prior Treatment with Enzalutamide or Abiraterone
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Infectious Disease Connect and ILÚM Health Solutions Combine to Advance Precision Treatment of Infectious Diseases and Antimicrobial Stewardship
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Merck Announces Appointment of Organon & Co. Chief Financial Officer and Chief Information Officer
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CORRECTING and REPLACING Merck Announces Appointment of Organon & Co. Chief Financial Officer and Chief Information Officer
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Merck to Present at the UBS Virtual Global Healthcare Conference
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Merck (MRK) New Combination Data for KEYTRUDA Demonstrated Clinical Benefit in Stage III NSCLC and Reinforce Long-Term Survival in Metastatic NSCLC
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Merck (MRK) KEYTRUDA Plus Chemotherapy Demonstrated Statistically Significant Improvement in Progression-Free Survival Versus Chemotherapy in Certain Patients with Metastatic Triple-Negative Breast Ca
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Merck's (MRK) KEYTRUDA Superior to Brentuximab Vedotin, a Standard of Care, in Patients With cHL in Head-to-Head Phase 3 Trial
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Merck (MRK) Novel HIF-2α Inhibitor Showed ORR of Nearly 30% in Patients with VHL Disease-Associated Clear Cell Renal Cell Carcinoma
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Merck’s Novel HIF-2α Inhibitor Showed an Objective Response Rate of Nearly 30% in Patients with von Hippel-Lindau (VHL) Disease-Associated Clear Cell Renal Cell Carcinoma
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Merck’s KEYTRUDA® (pembrolizumab) Superior to Brentuximab Vedotin (BV), a Standard of Care, in Patients With Classical Hodgkin Lymphoma (cHL) in Head-to-Head Phase 3 Trial
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Merck’s KEYTRUDA® (pembrolizumab) Plus Chemotherapy Demonstrated Statistically Significant Improvement in Progression-Free Survival Versus Chemotherapy in Certain Patients with Metastatic Triple-Ne
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New Combination Data for Merck’s KEYTRUDA® (pembrolizumab) Demonstrated Clinical Benefit in Stage III Non-Small Cell Lung Cancer (NSCLC) and Reinforce Long-Term Survival in Metastatic NSCLC
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Merck (MRK) Animal Health Reports Acquires U.S. Rights to SENTINEL Brand of Combination Parasiticides for Companion Animals
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Merck Animal Health to Acquire U.S. Rights to SENTINEL® Brand of Combination Parasiticides for Companion Animals
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Virbac to divest U.S. Rights to SENTINEL® brands to MSD Animal Health
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MilliporeSigma Granted U.S. Patents for Foundational CRISPR-Cas9 Technology
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LYNPARZA® (olaparib) Approved by FDA as First-Line Maintenance Treatment with Bevacizumab for HRD-Positive Advanced Ovarian Cancer
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Merck Announces Virtual 2020 Annual Shareholders Meeting
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Merck to Present at the BofA Securities 2020 Health Care Conference
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Merck to Present New Data from its Broad Oncology Portfolio and Pipeline at the ASCO20 Virtual Scientific Program
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Merck (MRK) Announces Results of Phase 3 Trial Evaluating RECARBRIO Versus Piperacillin and Tazobactam in Adult Patients with HABP/VABP Now Available
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Results of Phase 3 Trial Evaluating the Efficacy and Safety of Merck’s RECARBRIO™ (Imipenem, Cilastatin, and Relebactam) Versus Piperacillin and Tazobactam in Adult Patients with HABP/VABP Now Ava
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Merck Commits Additional $10 Million to COVID-19 Relief Efforts to Help Disparately Impacted Patients and Communities
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Merck (MRK) Announces FDA Approves KEYTRUDA for Use at Additional Recommended Dose of 400 mg Every Six Weeks for All Approved Adult Indications
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FDA Approves Merck’s KEYTRUDA® (pembrolizumab) for Use at an Additional Recommended Dose of 400 mg Every Six Weeks for All Approved Adult Indications
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Merck Announces First-Quarter 2020 Financial Results
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Merck (MRK) Announces First Clinical Outcomes Evaluating Six-Week Dosing Schedule for KEYTRUDA Presented at AACR
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First Clinical Outcomes Evaluating Six-Week Dosing Schedule for Merck’s KEYTRUDA® (pembrolizumab) Presented at AACR Virtual Annual Meeting I
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Merck (MRK), Institute for Systems Biology Collaborate to Define Molecular Mechanisms of SARS-CoV-2 Infection and Identify Potential Prognostic Biomarkers
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Merck and Institute for Systems Biology Collaborate to Define Molecular Mechanisms of SARS-CoV-2 Infection and Identify Potential Prognostic Biomarkers
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Merck (MRK) Announces LYNPARZA Demonstrated OS Benefit in Phase 3 PROfound Trial for BRCA1/2 or ATM-Mutated Metastatic Castration-Resistant Prostate Cancer
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LYNPARZA® (Olaparib) Demonstrated Overall Survival Benefit in Phase III PROfound Trial for BRCA1/2 or ATM-Mutated Metastatic Castration-Resistant Prostate Cancer
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LYNPARZA® (olaparib) Demonstrated Overall Survival Benefit in Phase 3 PROfound Trial for BRCA1/2 or ATM-Mutated Metastatic Castration-Resistant Prostate Cancer
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Merck (MRK) Resubmits sBLAs for KEYTRUDA Six-Week Dosing Schedule
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Merck Resubmits Supplemental Biologics License Applications (sBLAs) for KEYTRUDA® (pembrolizumab) Six-Week Dosing Schedule
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Merck Broadens Patient Support and Assistance Programs as Part of Overall COVID-19 Relief Efforts
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Merck (MRK) Reports US Launch of ONTRUZANT (trastuzumab-dttb), a Biosimilar of Herceptin® (trastuzumab)
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Merck Announces US Launch of ONTRUZANT® (trastuzumab-dttb), a Biosimilar of Herceptin® (trastuzumab)
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AstraZeneca (AZN), Merck (MRK) Announce KOSELUGO Approved by FDA for Pediatric Patients Two Years and Older With NF1 and Symptomatic, Inoperable PN
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KOSELUGO® (selumetinib) Approved by FDA for Pediatric Patients Two Years and Older With Neurofibromatosis Type 1 and Symptomatic, Inoperable Plexiform Neurofibromas
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Merck Announces $3M Commitment to Address Critical Maternal Health Needs During COVID-19 Pandemic
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Pfizer (PFE), EMD Serono Granted FDA Breakthrough Therapy Designation & Submit Application for BAVENCIO
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EMD Serono and Pfizer Receive US FDA Breakthrough Therapy Designation and Submit Application for BAVENCIO® for First-Line Maintenance Treatment of Locally Advanced or Metastatic Urothelial Carcinoma
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MilliporeSigma Awarded Second U.S. Patent for CRISPR Gene-Editing Technology

